The Role of B Cells and B Cell Therapies in Immune-Mediated Liver Diseases
Open accessAbstract
B cells form a branch of the adaptive immune system, essential for the body’s immune defense against pathogens. B cell dysfunction has been implicated in the pathogenesis of immune mediated liver diseases including autoimmune hepatitis, IgG4-related hepatobiliary disease, primary biliary cholangitis and primary sclerosing cholangitis. B cells may initiate and maintain immune related liver diseases in several ways including the production of autoantibodies and the activation of T cells via antigen presentation or cytokine production. Here we comprehensively review current knowledge on B cell mechanisms in immune mediated liver diseases, exploring disease pathogenesis, B cell therapies, and novel treatment targets. We identify key areas where future research should focus to enable the development of targeted B cell therapies.
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Plasma cells and plasmablasts extracted from the livers of patients with primary biliary cholangitis can secrete anti-mitochondrial antibodies with specificity for the lipoyl domains of PDC-E2.
“Plasma cells and plasmablasts extracted from the livers of patients with primary biliary cholangitis can secrete anti-mitochondrial antibodies with specificity for the lipoyl domains of PDC-E2.39”
From Primary biliary cholangitis. (2024) · cites this paper as [39]
The “Autoantibodies and B Cell Clonality in PBC” section reports that plasmablasts and plasma cells isolated from PBC livers produced anti-mitochondrial antibodies ex vivo, and identifies PDC-E2 as a major target of those antibodies. It does not specify that the antibodies produced by those isolated cells recognize the lipoyl domains of PDC-E2. (LLM, conf=0.88)
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Inverse Vaccination for Autoimmune Diseases: Insights into the Role of B Lymphocytes
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Immunomodulatory Roles of IL-15 in Immune Cells and its Potential for Cancer Immunotherapy
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Rituximab in Pemphigus Vulgaris: A Review of Monoclonal Antibody Therapy in Dermatology
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Autoimmune hepatitis: Towards a personalized treatment
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‘Can we cure IgG4-related diseases?’
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- Authors
- Cargill, T., & Culver, E. L.
- Affiliations
- University of Oxford (GB)
- John Radcliffe Hospital (GB)
- Corresponding author
- Culver, Emma L.
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2021-04-14
- Volume
- 12
- Pages
- 661196-661196
- ISSN
- 1664-3224 (ISSN-L)
- PMC
- PMC8079753
- OpenAlex
- W3153356633
- Cited by
- 46
- References
- 171
- Citations by year
- 2026: 8 · 2025: 8 · 2024: 14 · 2023: 7 · 2022: 6 · 2021: 3
- FWCI
- 0.98
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Immunology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Wellcome Trust (211042/Z/18/Z, 211042)
- National Institute for Health and Care Research (ACF-2015-13-007, 211042/Z/18/Z)
- University of Oxford
- Topics
- Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
- Health Sciences › Medicine › Rheumatology › IgG4-Related and Inflammatory Diseases
- Health Sciences › Medicine › Surgery › Pediatric Hepatobiliary Diseases and Treatments
- Keywords
- B cells, B cell dysfunction, immune-mediated liver disease, autoimmune hepatitis, primary biliary cirrhosis, primary sclerosing cholangitis, autoantibodies, T cell activation, antigen presentation, cytokine production, B-cell therapy, pathogenesis, treatment goals
- MeSH terms
- Animals, Autoantibodies, B-Lymphocytes, Clinical Trials as Topic, Humans, Immunoglobulin G, Immunotherapy, Liver, Liver Cirrhosis, Biliary, Liver Diseases, Cholangitis, Sclerosing, Hepatitis, Autoimmune, Mice
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